Miwa N - Search Results

1

Congenital arhinia: molecular-genetic analysis of five patients.

Sato D, Shimokawa O, Harada N, Olsen OE, Hou JW, Muhlbauer W, Blinkenberg E, Okamoto N, Kinoshita A, Matsumoto N, Kondo S, Kishino T, Miwa N, Ariga T, Niikawa N, Yoshiura K. Sato D, et al. Among authors: miwa n. Am J Med Genet A. 2007 Mar 15;143A(6):546-52. doi: 10.1002/ajmg.a.31613. Am J Med Genet A. 2007. PMID: 17304554

2

Genome-wide linkage analysis and mutation analysis of hereditary congenital blepharoptosis in a Japanese family.

Nakashima M, Nakano M, Hirano A, Kishino T, Kondoh S, Miwa N, Niikawa N, Yoshiura KI. Nakashima M, et al. Among authors: miwa n. J Hum Genet. 2008;53(1):34-41. doi: 10.1007/s10038-007-0214-6. Epub 2007 Nov 7. J Hum Genet. 2008. PMID: 17987257

3

Maternal isodisomy for 14q21-q24 in a man with diabetes mellitus.

Kayashima T, Katahira M, Harada N, Miwa N, Ohta T, Yoshiura K, Matsumoto N, Nakane Y, Nakamura Y, Kajii T, Niikawa N, Kishino T. Kayashima T, et al. Among authors: miwa n. Am J Med Genet. 2002 Jul 22;111(1):38-42. doi: 10.1002/ajmg.10511. Am J Med Genet. 2002. PMID: 12124731

4

The novel imprinted carboxypeptidase A4 gene ( CPA4) in the 7q32 imprinting domain.

Kayashima T, Yamasaki K, Yamada T, Sakai H, Miwa N, Ohta T, Yoshiura K, Matsumoto N, Nakane Y, Kanetake H, Ishino F, Niikawa N, Kishino T. Kayashima T, et al. Among authors: miwa n. Hum Genet. 2003 Mar;112(3):220-6. doi: 10.1007/s00439-002-0891-3. Epub 2003 Jan 28. Hum Genet. 2003. PMID: 12552318

5

A strong association of axillary osmidrosis with the wet earwax type determined by genotyping of the ABCC11 gene.

Nakano M, Miwa N, Hirano A, Yoshiura K, Niikawa N. Nakano M, et al. Among authors: miwa n. BMC Genet. 2009 Aug 4;10:42. doi: 10.1186/1471-2156-10-42. BMC Genet. 2009. PMID: 19650936 Free PMC article.

6

Identification, characterization and mapping of the human ZIS (zinc-finger, splicing) gene.

Nakano M, Yoshiura K, Oikawa M, Miyoshi O, Yamada K, Kondo S, Miwa N, Soeda E, Jinno Y, Fujii T, Niikawa N. Nakano M, et al. Among authors: miwa n. Gene. 1998 Dec 28;225(1-2):59-65. doi: 10.1016/s0378-1119(98)00536-8. Gene. 1998. PMID: 9931435

7

A SNP in the ABCC11 gene is the determinant of human earwax type.

Yoshiura K, Kinoshita A, Ishida T, Ninokata A, Ishikawa T, Kaname T, Bannai M, Tokunaga K, Sonoda S, Komaki R, Ihara M, Saenko VA, Alipov GK, Sekine I, Komatsu K, Takahashi H, Nakashima M, Sosonkina N, Mapendano CK, Ghadami M, Nomura M, Liang DS, Miwa N, Kim DK, Garidkhuu A, Natsume N, Ohta T, Tomita H, Kaneko A, Kikuchi M, Russomando G, Hirayama K, Ishibashi M, Takahashi A, Saitou N, Murray JC, Saito S, Nakamura Y, Niikawa N. Yoshiura K, et al. Among authors: miwa n. Nat Genet. 2006 Mar;38(3):324-30. doi: 10.1038/ng1733. Epub 2006 Jan 29. Nat Genet. 2006. PMID: 16444273

8

Involvement of claudin-1 in the beta-catenin/Tcf signaling pathway and its frequent upregulation in human colorectal cancers.

Miwa N, Furuse M, Tsukita S, Niikawa N, Nakamura Y, Furukawa Y. Miwa N, et al. Oncol Res. 2001;12(11-12):469-76. doi: 10.3727/096504001108747477. Oncol Res. 2001. PMID: 11939410

9

AXIN1 mutations in hepatocellular carcinomas, and growth suppression in cancer cells by virus-mediated transfer of AXIN1.

Satoh S, Daigo Y, Furukawa Y, Kato T, Miwa N, Nishiwaki T, Kawasoe T, Ishiguro H, Fujita M, Tokino T, Sasaki Y, Imaoka S, Murata M, Shimano T, Yamaoka Y, Nakamura Y. Satoh S, et al. Among authors: miwa n. Nat Genet. 2000 Mar;24(3):245-50. doi: 10.1038/73448. Nat Genet. 2000. PMID: 10700176

10

Isolation of a novel human gene, APCDD1, as a direct target of the beta-Catenin/T-cell factor 4 complex with probable involvement in colorectal carcinogenesis.

Takahashi M, Fujita M, Furukawa Y, Hamamoto R, Shimokawa T, Miwa N, Ogawa M, Nakamura Y. Takahashi M, et al. Among authors: miwa n. Cancer Res. 2002 Oct 15;62(20):5651-6. Cancer Res. 2002. PMID: 12384519

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